Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052724Generated: November 3, 2026

Cesium fluoride → (S)-4-Amino-N-(3-fluoro-5-hydroxyphenyl)-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/1052724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-6-bromo-N-(3-fluoro-5-hydroxyphenyl)pyrimidine-5-carboxamideHCID 90102165—
Reactant(S)-2-(1-Aminoethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-oneHCID 90102580—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product(S)-4-Amino-N-(3-fluoro-5-hydroxyphenyl)-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidine-5-carboxamideHCID 737759328%

Reaction Conditions

Temperature120 °C

Reaction Steps

(S)-2-(1-Aminoethyl)-5-methyl-3-phenylpyrrolo[2,1-f][1,2,4]triazin-4(3H)-one (100 mg, 0.37 mmol), 4-amino-6-bromo-N-(3-fluoro-5-hydroxyphenyl)pyrimidine-5-carboxamide (183 mg, 0.56 mmol), DIEA (325 μl, 1.87 mmol) and cesium fluoride (113 mg, 0.74 mmol) were suspended in tert-butanol (5 ml) and the mixture was stirred overnight at 120° C. in a sealed tube. The reaction mixture was diluted with ethyl acetate and washed with water and brine. After evaporation of the solvent, the residue was purified by reverse phase using SP1® Purification System to give 15 mg (8% yield) as a solid. Purity 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388189B2
Source datasetuspto-grants-2016_07
ORD IDord-0a28a87741384c10a26937123d028bed
Source noteuspto-grants-2016_07